The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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21476–21500 of 90018

  • HighFDA (Food)·F-0327-2023·2023-02-08

    Frozen breakfast sandwiches and burritos recalled for undeclared milk allergen

    The Miso Brothers Inc. is recalling frozen breakfast sandwiches and breakfast burritos containing undeclared milk, affecting approximately 31,092 units distributed throughout US retail locations. This poses a risk to consumers with milk allergies.

    Product
    Alpha Plant-Based Breakfast Sandwich - Meatless Sausage, Plant-Based Egg & Cheeze 5 oz. UPC 810070350093 Frozen
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1032-2023·2023-02-08

    Non-sterile procedural trays with potential sterile packaging breach

    Medline Industries is recalling non-sterile procedural trays containing sterile blades that may damage sterile packaging due to blade puncture risk. Lot 22IBQ980. No illnesses reported.

    Product
    Non-sterile procedural trays labeled as MAJOR/MINOR, 3 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0326-2023·2023-02-08

    Plant-based breakfast burritos recalled for undeclared milk allergen

    THE MISO BROTHERS INC is recalling 31,092 units of frozen Alpha Plant Based Breakfast Burritos due to undeclared milk. The product may contain milk, a common allergen.

    Product
    Alpha Plant Based Breakfast Burrito - Meatless Sausage SCRAMBLE 5.5 oz UPC 855099007733 Frozen
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1048-2023·2023-02-08

    GORE CARDIOFORM Septal Occluder Recalled for Incomplete Quality Documentation

    W L Gore & Associates is recalling 14 units of the GORE CARDIOFORM Septal Occluder (GSX0030A) due to incomplete quality test documentation. The missing verification of device release could pose a potential risk of device failure and serious complications.

    Product
    GORE CARDIOFORM Septal Occluder, REF: GSX0030A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-02082023-01·2023-02-08

    Goulart's Smoked Linguica Links Recalled for Undeclared Milk Allergen

    USDA FSIS issued a public health alert for Goulart's Smoked Linguica Links due to undeclared milk. Consumers with dairy allergies should not consume these products.

    Product
    Goulart's Sausage Co. — FSIS Issues Public Health Alert for Ready-To-Eat Pork Sausage Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0262-2023·2023-02-08

    Diltiazem Hydrochloride extended-release capsules recalled due to failed quality specifications

    Sun Pharmaceutical is recalling Diltiazem Hydrochloride Extended-Release Capsules (360 mg) due to failed impurity specifications and dissolution testing found during FDA laboratory evaluation. The recall affects five lot numbers distributed nationwide.

    Product
    DILTIAZEM HYDROCHLORIDE — DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1022-2023·2023-02-08

    SynCardia Total Artificial Heart System Recalled for Cannula Tears

    SynCardia Systems is recalling its Total Artificial Heart System due to reported tears in the cannula caused by wear and tear stress. Approximately 1,732 systems worldwide are affected.

    Product
    SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1038-2023·2023-02-08

    Turbett Surgical Container TS1000 may have weld failures breaching sterile barrier

    Turbett Surgical Container TS1000 may have weld failures that breach the sterile barrier, potentially resulting in unsterile instruments being used in medical procedures and risking patient infection or injury.

    Product
    Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1047-2023·2023-02-08

    Medline UNITE Foot & Ankle Drill Bit Recalled for Intra-operative Screw Failure Risk

    Medline Industries recalls 190 UNITE foot and ankle drill bits due to observed screw failure during surgery. When used to pre-drill holes for certain screw sizes, the drill bits may fail under surgical torque, creating risk during procedures.

    Product
    MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1030-2023·2023-02-08

    Non-sterile procedural trays risk sterile packaging breach

    Medline Industries is recalling non-sterile laparoscopic procedural trays containing sterile blades that may puncture the outer packaging, potentially breaching the sterile barrier. 260 cases have been distributed nationwide.

    Product
    Non-sterile procedural trays labeled as LAPAROSCOPIC, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1029-2023·2023-02-08

    MEDLINE procedural trays recalled for potential sterile packaging breach

    MEDLINE is recalling procedural trays because sterile blades within the kits could puncture the outer foil packaging, potentially breaching the sterile barrier.

    Product
    Non-sterile procedural trays labeled as CRANI, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·23115·2023-02-08

    Fabuloso Multi-Purpose Cleaners Recalled for Bacterial Contamination Risk

    Colgate-Palmolive is recalling about 4.9 million Fabuloso Multi-Purpose Cleaners due to contamination with Pseudomonas bacteria. People with weakened immune systems, external medical devices, or underlying lung conditions face a risk of serious infection from exposure.

    Product
    Fabuloso Multi-Purpose Cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0339-2023·2023-02-08

    Daim Swedish Almond Cake Recalled for Metal Contamination

    Almondy AB is recalling Daim Swedish almond cake (NET WT 14.1oz) due to discovery of a metal object in the product. Consumers should not eat affected cakes.

    Product
    Daim, Swedish almond cake with chocolate and crunchy caramel, Baked by Almondy, NET WT 14.1oz (400g)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1027-2023·2023-02-08

    Temperature Monitoring Adapter Detachment in Cardiopulmonary Bypass Oxygenators

    Medtronic is recalling cardiopulmonary bypass equipment because the Temperature Monitoring Adapter can come loose during setup or disassembly, potentially compromising temperature monitoring during heart surgery.

    Product
    Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, REF BB811. Used in Cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1043-2023·2023-02-08

    Biomet Vanguard Knee Implant Components Recalled for Incorrect Labeling

    Biomet, Inc. is recalling specific Vanguard Knee System prosthetic components that are incorrectly labeled with wrong sizes and sides. This labeling error could result in incorrect implant placement during knee replacement surgery.

    Product
    (1) Vanguard Knee System PS Open Box Femoral; Left; 57.5 mm. Intended for Knee joint replacement prostheses. Item Number: 183122 EXPANDED RECALL: (2) Vanguard Knee System PS Open Box Femoral; Left; 60 mm. Item Number: 183124 (3) Vanguard Knee System PS Open Box Femoral…
    Category
    Medical Device
    Distribution
    6 states
  • HighNHTSA·23V056000·2023-02-07

    Pleasant Valley Teardrop Trailers Recalled for Gas Leak Risk

    Pleasant Valley is recalling 2023 Teardrop TAB 320s and TAB 320CSS travel trailers because internal aluminum burner tubes may fracture, causing a gas leak that could lead to fire.

    Product
    PLEASANT VALLEY — PLEASANT VALLEY TEARDROP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V057000·2023-02-07

    Maintainer Service Trucks Recalled for Uncontrolled Crane Movement Risk

    Maintainer is recalling 2019-2023 service trucks with hydraulic cranes because power loss may cause uncontrolled movement, increasing injury risk.

    Product
    MAINTAINER — MAINTAINER CRANE W/ SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E008000·2023-02-07

    Lippert Recalls RV Entry Door Latches Due to Failure Risk

    Lippert is recalling specific RV entry door latches that may fail, preventing entry or exit. This defect increases the risk of injury during an emergency.

    Product
    LATCHES/LOCKS/LINKAGES:DOORS:LATCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V054000·2023-02-06

    Nova Bus Recalls 2022 LFS Transit Buses for Steering Hose Defect

    Nova Bus is recalling 2022 LFS transit buses because the power steering hose may not have been assembled correctly, which can result in hose detachment and a loss of power steering assist.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E007000·2023-02-06

    Tokai Rika Seat Belt Assemblies Recalled for Force-Limiter Defect

    Tokai Rika is recalling certain front-seat outer right-side seat belt assemblies because the force-limiter may not operate correctly. This defect could allow the belt to extend further than intended, increasing injury risk in a crash.

    Product
    SEAT BELTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V053000·2023-02-05

    2022 Can-Am Spyder F3 Recalled for Rearview Mirror Lens Detachment

    Bombardier is recalling 2022 Can-Am Spyder F3 and F3-S motorcycles because the rearview mirror lens may detach, reducing rear visibility and increasing crash risk.

    Product
    CAN-AM — CAN-AM SPYDER F3-S, SPYDER F3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V052000·2023-02-04

    Nexus RVs Recalls 2022 Motorhomes Due to Awning Seam Separation Risk

    Nexus RVs is recalling 2022 motorhomes because a welded seam on the electric retractable awning may separate, potentially allowing the awning to drop and increase the risk of injury.

    Product
    NEXUS — NEXUS GHOST, WRAITH, VERRADO, REBEL 4X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·004-2023·2023-02-03

    USDA Recalls Ineligible Frozen Catfish Imported from India

    Delight Foods USA LLC and Delight Foods LLC are recalling approximately 2,961 pounds of frozen catfish imported from India because the country is ineligible to export these products to the U.S.

    Product
    Delight Foods USA LLC Recalls Ineligible Frozen Siluriformes Products Imported from India
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V050000·2023-02-03

    BMW Recalls 2023 760i and i7 Models Due to Airbag Software Defect

    BMW is recalling 397 vehicles because a software error may disable front passenger airbags and active headrests, increasing injury risk in crashes.

    Product
    BMW — BMW 760I, I7
    Category
    Vehicle
    Distribution
    Distributed nationwide